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Structure of 69454-42-8
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Methyl 1-oxo-1,2-dihydroisoquinoline-3-carboxylate features a rigid, electron-deficient isoquinoline core that enables direct functionalization at the C3 position. This bench-stable scaffold integrates readily into synthetic sequences requiring planar heterocyclic motifs. The ester group facilitates downstream derivatization while maintaining compatibility with standard coupling conditions.
Methyl 1-oxo-1,2-dihydroisoquinoline-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to isoquinoline-based scaffolds. Its conjugated enone system facilitates nucleophilic addition and Michael-type reactions, while the ester group supports further functionalization via hydrolysis or reduction. The compound exhibits good bench stability and compatibility with standard reaction conditions, making it well-suited for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: